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A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

A man experienced hair loss from radiotherapy, which can be temporary or permanent depending on radiation dose, with potential treatments available.

The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

AB+ blood group is more common in alopecia areata patients.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

Certain gene variations in the Vitamin D Receptor are linked to higher risk of female hair loss.

Lacking cyclin D3 reduces skin cancer growth without affecting normal skin cell growth.

Six genetic conditions are often linked to complete scalp hair loss in children.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Understanding hair growth involves complex factors, and more research is needed to improve treatments for hair loss conditions.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Certain skin proteins can form anchoring structures without the protein AMACO.

Hypothyroidism may cause certain types of hair loss.

Two specific genetic markers increase the risk of hair loss in Asian populations.

New genes linked to male pattern baldness were found on chromosome 20p11.

A patient with a rare chromosome condition also had a rare type of hair loss.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

The document concludes that more multidisciplinary research is needed to understand and treat PCOS, a condition that significantly affects women's health and quality of life.

Sheep have a unique gene, KAP8-2, that humans don't have, which may affect wool properties.

New treatments for alopecia areata may target specific immune cells and pathways involved in hair loss.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

The meeting discussed various skin conditions, treatments, and unusual cases, highlighting the effectiveness of tetracycline in treating rosacea.